CNR Institutional Research Information System

D'ESPOSITO, MAURIZIO
 Distribuzione geografica
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Continente #
AS - Asia 2.521
NA - Nord America 1.386
EU - Europa 622
SA - Sud America 466
AF - Africa 59
Totale 5.054
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Nazione #
US - Stati Uniti d'America 1.314
SG - Singapore 1.081
CN - Cina 516
BR - Brasile 377
HK - Hong Kong 307
VN - Vietnam 233
IT - Italia 193
FR - Francia 151
KR - Corea 106
BD - Bangladesh 92
DE - Germania 69
NL - Olanda 65
IN - India 41
CA - Canada 36
GB - Regno Unito 36
JP - Giappone 34
AR - Argentina 26
FI - Finlandia 20
ZA - Sudafrica 19
MX - Messico 18
ID - Indonesia 15
IQ - Iraq 15
TR - Turchia 15
EC - Ecuador 14
CL - Cile 13
PL - Polonia 12
MA - Marocco 10
PY - Paraguay 10
SA - Arabia Saudita 10
CO - Colombia 9
IL - Israele 9
RU - Federazione Russa 9
UZ - Uzbekistan 9
ES - Italia 8
VE - Venezuela 8
AT - Austria 7
UA - Ucraina 7
CZ - Repubblica Ceca 6
EG - Egitto 6
GR - Grecia 5
LT - Lituania 5
PK - Pakistan 5
AZ - Azerbaigian 4
DZ - Algeria 4
IE - Irlanda 4
JM - Giamaica 4
JO - Giordania 4
KE - Kenya 4
MY - Malesia 4
SE - Svezia 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
BO - Bolivia 3
CR - Costa Rica 3
KZ - Kazakistan 3
RO - Romania 3
TH - Thailandia 3
TN - Tunisia 3
BW - Botswana 2
CH - Svizzera 2
ET - Etiopia 2
GT - Guatemala 2
GY - Guiana 2
HN - Honduras 2
HR - Croazia 2
HU - Ungheria 2
KG - Kirghizistan 2
KW - Kuwait 2
LB - Libano 2
PE - Perù 2
RS - Serbia 2
UY - Uruguay 2
ZM - Zambia 2
AM - Armenia 1
AO - Angola 1
BE - Belgio 1
BG - Bulgaria 1
CG - Congo 1
CI - Costa d'Avorio 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GD - Grenada 1
KH - Cambogia 1
LV - Lettonia 1
MD - Moldavia 1
ML - Mali 1
MM - Myanmar 1
MU - Mauritius 1
NG - Nigeria 1
NI - Nicaragua 1
PH - Filippine 1
PS - Palestinian Territory 1
PT - Portogallo 1
SC - Seychelles 1
SI - Slovenia 1
SV - El Salvador 1
TC - Turks e Caicos 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
VG - Isole Vergini Britanniche 1
Totale 5.054
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Città #
Singapore 648
Santa Clara 378
Hong Kong 303
Hefei 211
San Jose 135
Ashburn 121
Lauterbourg 115
Seoul 103
Ho Chi Minh City 101
Los Angeles 88
Beijing 87
Hanoi 54
Frankfurt am Main 44
Naples 40
Dallas 34
New York 32
São Paulo 32
Buffalo 29
Tokyo 20
Rome 19
Avellino 13
Curitiba 12
Orem 12
Rio de Janeiro 12
Brooklyn 11
Turners Falls 11
Atlanta 10
Aversa 10
Helsinki 10
Milan 10
Minamishinagawa 10
Haiphong 9
Montreal 9
Tashkent 9
Baghdad 8
Chennai 8
Da Nang 8
Denver 8
Guangzhou 8
Johannesburg 8
London 8
Manchester 8
Toronto 8
Brasília 7
Campinas 7
Chicago 7
Dhaka 7
Fortaleza 7
San Francisco 7
Warsaw 7
Amsterdam 6
Belo Horizonte 6
Bologna 6
Jeddah 6
Munich 6
Phoenix 6
Turku 6
Athens 5
Cairo 5
Cleveland 5
Istanbul 5
Malang 5
Newark 5
Porto Alegre 5
Redondo Beach 5
Turin 5
Amman 4
Asunción 4
Baku 4
Bari 4
Bengaluru 4
Boston 4
Cape Town 4
Dublin 4
Düsseldorf 4
Elk Grove Village 4
Franca 4
Goiânia 4
Guayaquil 4
Karachi 4
Lappeenranta 4
Mauá 4
Nairobi 4
Ninh Bình 4
Osasco 4
Quảng Ngãi 4
Santiago 4
Stockholm 4
Teresina 4
Vienna 4
Betim 3
Bogotá 3
Buenos Aires 3
Bắc Ninh 3
Campos dos Goytacazes 3
Caracas 3
Casablanca 3
Caxias do Sul 3
Divinópolis 3
Hanover 3
Totale 3.076
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Nome #
Epigenetic control of hypoxia inducible factor-1?-dependent expression of placental growth factor in hypoxic conditions 101
X inactivation and reactivation in X-linked diseases 97
Deep Insights Into Mecp2-Driven Transcriptional (De)Regulation At Embryonic Developmental Stage Through RNA-Seq Data Analysis 94
The evolutionary history of the second pseudoautosomal region revised 90
F(2)-dihomo-isoprostanes as potential early biomarkers of lipid oxidative damage in Rett syndrome 81
MULTI-OMICS ANALYSIS SHEDS LIGHT ON HOW SHELF-LIFE OF TOMATO FRUIT IS PROLONGED 79
Multi-omics data integration provides insights into the post-harvest biology of a long shelf-life tomato landrace 73
F(4)-neuroprostanes mediate neurological severity in Rett syndrome. 69
Glycosphingolipid metabolic reprogramming drives neural differentiation 68
Alternative splicing of the human gene SYBL1 modulates protein domain architecture of longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms. 62
Genomic and epigenomic analysis of tomato fruit senescence 61
Select item 10671Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online. 60
Agonist stimulated 5-HT7R recovers gene expression profile in cortical neurons of a Rett syndrome mouse model 60
A dual mechanism controlling the localization and function of exocytic v-SNAREs 58
Global transcriptome profiles of italian mediterranean buffalo embryos with normal and retarded growth. 57
Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome 57
GENOME-WIDE ANALYSIS OF HISTONE MODIFICATIONS AND ASSOCIATION WITH RIPENING-RELATED GENES DURING POST-HARVEST IN TOMATO FRUIT 57
CODING AND NON-CODING RNAS IN A LONG SHELF-LIFE TOMATO VARIETY 56
Genetic variability at the second pseudoautosomal region in ancient and modern humans 56
Minimally Invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 55
MECP2, a multi-talented modulator of chromatin architecture 55
ZFP57/KAP1 Genomic Association and Targeted Epigenetic Regulation at Imprinted and Not Imprinted Loci 55
O6-methylguanine-DNA methyltransferase in equine sarcoids: molecular and epigenetic analysis. 54
INSIGHTS INTO FRUIT SENESCENCE REGULATORY NETWORKS IN A TOMATO LANDRACE WITH LONG SHELF-LIFE 54
DNA methylation in X inactivation, imprinting and associated diseases 53
A Multi-Omics approach to get insights into fruit senescence regulatory networks in a tomato landrace with long shelf-life. 53
Transcriptomic and epigenomic landscape in rett syndrome 52
Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling 52
Vamp7 51
In vivo analysis of DNA methylation patterns recognized by specific proteins: coupling chromatin immunoprecipitation and bisulfite genomic sequencing 50
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 49
The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients 49
Early oxidative damage in Rett mouse brain 48
Genomic characterization and chromosomal mapping of 5 river buffalo skeletal muscle differentiation master genes 47
Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome 46
Multi-Omics analysis of tomato fruit senescence 45
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing. 45
Human synaptobrevin like 1 gene basal transcription is regulated through the interaction of Staf-ZNF143 factors with evolutionary conserved Cis-elements 44
Differential DNA Methylation as a Tool for Non-Invasive Prenatal Diagnosis (NIPD) of X Chromosome Aneuploidies 43
DDX11L: a novel transcript family emerging from human subtelomeric regions 43
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome 43
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 43
Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region 43
Partial rescue of Rett syndrome by omega-3 polyunsaturated fatty acids (PUFAs) oil 42
Reduced brain UCP2 expression mediated by microRNA-503 contributes to increased stroke susceptibility in the high-salt fed stroke-prone spontaneously hypertensive rat 42
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 42
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 41
Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease. 41
Epigenetic regulation of hypoxia-induced PlGF expression 40
An autoregulatory loop mediated by miR-21 and PDCD4 controls the AP-1 activity in RAS transformation 40
Non-coding RNAs in chromatin disease involving neurological defects 40
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications 39
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome. 39
From sequence analysis to diseases identification in the distal human xq28 39
Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome 39
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 39
Expressed STSs and transcription of human Xq28. 38
VAMP subfamilies identified by specific R-SNARE motifs 38
MECP2 Duplication Syndrome: Evidence of Enhanced Oxidative Stress. A Comparison with Rett Syndrome 38
Longins and their longins domains:regulated SNAREs and multifunctional SNARE regulators 38
Molecular and epigenetic analysis of the fragile histidine triad tumour suppressor gene in equine sarcoids 38
Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia. 37
Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease 36
Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome 36
Anti-Mullerian hormone (AMH) concentration in follicular fluid and mRNA expression of AMH receptor type II and LH receptor in granulosa cells as predictive markers of good buffalo (Bubalus bubalis) donors 35
Physical mappaing of a retinal-specific trascription factor and the epigenetic mark H3K9me3 correlated to rhodopsin and genome wide retinal loci. 35
Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2) 34
Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes. 34
Role of Mecp2 in the High-Order Chromatin Structure During Neural Differentiation 33
Expression of HOX homeogenes in human neuroblastoma cell culture lines. 33
Chromosome territory re-organisation in a human disease with altered DNA methylation 33
Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples 32
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 32
Molecular analysis of the heterogeneity region of the human ribosomal spacer. 32
Relationships between MeCP2 and pericentric heterochromatin factors during neural differentiation 32
The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site. 32
MeCP2 as a genome-wide modulator: the renewal of an old story. 32
Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype. 31
Chapter 18. Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 31
Expression of HOX homeogenes in human neuroblastoma cell culture lines 31
Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts 31
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications 30
MeCP2 transcription analysis and X-inactivation pattern in a Rett girl brain tissue. 29
DNA methylation 40 years later: its role in human health and disease 29
Epigenetic control of hypoxia-induced Placental Growth Factor expression 29
Partial rescue of Rett syndrome by omega-3 polyunsaturated fatty acids (PUFAs) oil 28
Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome. 28
Molecular dissection of two human chromatin disease, Rett syndrome and ICF syndrome 28
Epigenomic and transcriptional effects of Dnmt3b mutations in human ICF syndrome-derived B cell lines. 27
MeCP2 is required for major satellite forward transcript recruitment at pericentric heterochromatin during neural differentiation 27
Two human homeobox genes. c1 and c8: structure analysis and expression in embryonic development. 27
Second Human Peudoautosomal Region: Biology, Genes and Implication for the Pathogenesis of Rett Syndrome 27
DNA METHYLATION IN TRANSCRIPTIONAL REPRESSION OF TWO DIFFERENTIALLY EXPRESSED X-LINKED GENES, GPC3 AND SYBL1 27
Involvement of HIF-1alfa in hypoxia-induced Placental Growth Factor expression 26
Scavenger Receptor B1 oxidative post-translational modifications are responsible for its loss in Rett syndrome 26
EPITOM: an integrated study of epigenomics in tomato fruit during post-harvest 26
A serine 37 mutation associated with two missense mutations at highly conserved regions of p53 affect pro-apoptotic genes expression in a T-lymphoblastoid drug resistant cell line 26
Molecular cloning and characterization of the clock gene period2 in the testis of lizard Podarcis sicula and its expression during seasonal reproductive cycle 25
Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant 25
Subclinical myocardial dysfunction in Rett syndrome 25
Totale 4.398
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Categoria #
all - tutte 17.233
article - articoli 12.173
book - libri 77
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 465
Totale 29.948
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202431 0 0 0 0 0 0 0 0 2 0 28 1
2024/20251.810 32 9 150 75 347 51 8 88 51 80 494 425
2025/20263.112 157 256 278 474 525 167 472 150 147 179 152 155
2026/2027116 116 0 0 0 0 0 0 0 0 0 0 0
Totale 5.069